63807-86-3 Usage
Description
Used in Pharmaceutical Industry:
Sappanone A is used as a therapeutic agent for various conditions due to its potential to inhibit the activity of enzymes involved in inflammation. It is being studied for its potential use in the treatment of cancer, diabetes, and cardiovascular disease.
Used in Antimicrobial Applications:
Sappanone A is used as an antimicrobial agent because of its ability to combat microbial infections, making it a promising candidate for the development of new pharmaceutical compounds.
Used in Antiviral Applications:
Sappanone A is used as an antiviral agent, exhibiting potential in the development of new pharmaceuticals to combat viral infections.
Check Digit Verification of cas no
The CAS Registry Mumber 63807-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63807-86:
(7*6)+(6*3)+(5*8)+(4*0)+(3*7)+(2*8)+(1*6)=143
143 % 10 = 3
So 63807-86-3 is a valid CAS Registry Number.
63807-86-3Relevant articles and documents
SYNTHESIS OF ERYTHRININ A, A NATURALLY OCCURING PYRANOISOFLAVONE
Suresh, R. V.,Iyer, C. S. Rukmani,Iyer, P. R.
, p. 2479 - 2482 (2007/10/02)
Erythrinin A (10) has been synthesised by the oxidative rearrangement of dihydropyranochalcone 1 with thallium(III)nitrate (TTN) in trimethyl orthoformate (TMOF) to the dimethyl acetal 2, followed by cyclisation to 3, demethylation to 6 and dehydrogenation.Compound 10 could also be obtained from chalcone 4 on similar rearrangement followed by cyclisation, demethoxymethylation and dehydrogenation.In another route, chalcone 7 was oxidatively rearranged with TTN in TMOF, to 8 which on treatment with HCl yielded 10.
Synthesis of Erythrinin-A and Related Isoflavones
Jain, A. C.,Gupta, S.,Gupta, A.,Bambah, P.
, p. 609 - 613 (2007/10/02)
Erythrinin-A (1) is best synthesized by the condensation of 6-acetyl-7-hydroxy-2,2-dimethylchroman (15) with p-methoxymethoxybenzaldehyde in the presence of alkali followed by oxidative rearrangement of the resulting chalcone (16) with Tl(NO3)3 in MeOH, d